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Previous release (v1)
2024-04-24 03:29:33, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_012129 3490 bp mRNA linear PRI 18-DEC-2022 DEFINITION Homo sapiens claudin 12 (CLDN12), transcript variant 3, mRNA. ACCESSION NM_012129 VERSION NM_012129.5 KEYWORDS RefSeq. SOURCE Homo sapiens (human) ORGANISM Homo sapiens Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo. REFERENCE 1 (bases 1 to 3490) AUTHORS Kolchakova D, Moten D, Batsalova T and Dzhambazov B. TITLE Tight Junction Protein Claudin-12 Is Involved in Cell Migration during Metastasis JOURNAL Biomolecules 11 (5), 636 (2021) PUBMED 33922921 REMARK GeneRIF: Tight Junction Protein Claudin-12 Is Involved in Cell Migration during Metastasis. Publication Status: Online-Only REFERENCE 2 (bases 1 to 3490) AUTHORS Rahman A, Kobayashi M, Sugimoto K, Endo Y, Kojima M, Furukawa S, Watanabe T, Soeda S, Hashimoto Y, Fujimori K and Chiba H. TITLE Reduced Claudin-12 Expression Predicts Poor Prognosis in Cervical Cancer JOURNAL Int J Mol Sci 22 (7), 3774 (2021) PUBMED 33917356 REMARK GeneRIF: Reduced Claudin-12 Expression Predicts Poor Prognosis in Cervical Cancer. Publication Status: Online-Only REFERENCE 3 (bases 1 to 3490) AUTHORS Luck K, Kim DK, Lambourne L, Spirohn K, Begg BE, Bian W, Brignall R, Cafarelli T, Campos-Laborie FJ, Charloteaux B, Choi D, Cote AG, Daley M, Deimling S, Desbuleux A, Dricot A, Gebbia M, Hardy MF, Kishore N, Knapp JJ, Kovacs IA, Lemmens I, Mee MW, Mellor JC, Pollis C, Pons C, Richardson AD, Schlabach S, Teeking B, Yadav A, Babor M, Balcha D, Basha O, Bowman-Colin C, Chin SF, Choi SG, Colabella C, Coppin G, D'Amata C, De Ridder D, De Rouck S, Duran-Frigola M, Ennajdaoui H, Goebels F, Goehring L, Gopal A, Haddad G, Hatchi E, Helmy M, Jacob Y, Kassa Y, Landini S, Li R, van Lieshout N, MacWilliams A, Markey D, Paulson JN, Rangarajan S, Rasla J, Rayhan A, Rolland T, San-Miguel A, Shen Y, Sheykhkarimli D, Sheynkman GM, Simonovsky E, Tasan M, Tejeda A, Tropepe V, Twizere JC, Wang Y, Weatheritt RJ, Weile J, Xia Y, Yang X, Yeger-Lotem E, Zhong Q, Aloy P, Bader GD, De Las Rivas J, Gaudet S, Hao T, Rak J, Tavernier J, Hill DE, Vidal M, Roth FP and Calderwood MA. TITLE A reference map of the human binary protein interactome JOURNAL Nature 580 (7803), 402-408 (2020) PUBMED 32296183 REFERENCE 4 (bases 1 to 3490) AUTHORS Huang J, Yin P and Zhang L. TITLE COPII cargo claudin-12 promotes hepatitis C virus entry JOURNAL J Viral Hepat 26 (2), 308-312 (2019) PUBMED 30339745 REMARK GeneRIF: We found that COPII cargo CLDN12 is important for Hepatitis C Virus entry. REFERENCE 5 (bases 1 to 3490) AUTHORS Sweeney MD, Zhao Z, Montagne A, Nelson AR and Zlokovic BV. TITLE Blood-Brain Barrier: From Physiology to Disease and Back JOURNAL Physiol Rev 99 (1), 21-78 (2019) PUBMED 30280653 REMARK Review article REFERENCE 6 (bases 1 to 3490) AUTHORS Kiuchi-Saishin Y, Gotoh S, Furuse M, Takasuga A, Tano Y and Tsukita S. TITLE Differential expression patterns of claudins, tight junction membrane proteins, in mouse nephron segments JOURNAL J Am Soc Nephrol 13 (4), 875-886 (2002) PUBMED 11912246 REFERENCE 7 (bases 1 to 3490) AUTHORS Niimi T, Nagashima K, Ward JM, Minoo P, Zimonjic DB, Popescu NC and Kimura S. TITLE claudin-18, a novel downstream target gene for the T/EBP/NKX2.1 homeodomain transcription factor, encodes lung- and stomach-specific isoforms through alternative splicing JOURNAL Mol Cell Biol 21 (21), 7380-7390 (2001) PUBMED 11585919 REFERENCE 8 (bases 1 to 3490) AUTHORS Tsukita S, Furuse M and Itoh M. TITLE Multifunctional strands in tight junctions JOURNAL Nat Rev Mol Cell Biol 2 (4), 285-293 (2001) PUBMED 11283726 REMARK Review article REFERENCE 9 (bases 1 to 3490) AUTHORS Heiskala M, Peterson PA and Yang Y. TITLE The roles of claudin superfamily proteins in paracellular transport JOURNAL Traffic 2 (2), 93-98 (2001) PUBMED 11247307 REMARK Review article REFERENCE 10 (bases 1 to 3490) AUTHORS Kniesel U and Wolburg H. TITLE Tight junctions of the blood-brain barrier JOURNAL Cell Mol Neurobiol 20 (1), 57-76 (2000) PUBMED 10690502 REMARK Review article COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AC006153.2. On May 31, 2019 this sequence version replaced NM_012129.4. Summary: This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. This gene is expressed in the inner ear and bladder epithelium, and it is over-expressed in colorectal carcinomas. This protein and claudin 2 are critical for vitamin D-dependent Ca2+ absorption between enterocytes. Multiple alternatively spliced transcript variants encoding the same protein have been found.[provided by RefSeq, Sep 2011]. Transcript Variant: This variant (3) lacks an exon in the 5' UTR, as compared to variant 1. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: SRR7346977.1967800.1, BC068532.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1966682 [ECO:0000348] ##Evidence-Data-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-89 AC006153.2 39720-39808 90-179 AC006153.2 41778-41867 180-3490 AC006153.2 48903-52213 FEATURES Location/Qualifiers source 1..3490 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="7" /map="7q21.13" gene 1..3490 /gene="CLDN12" /note="claudin 12" /db_xref="GeneID:9069" /db_xref="HGNC:HGNC:2034" /db_xref="MIM:611232" exon 1..89 /gene="CLDN12" /inference="alignment:Splign:2.1.0" variation 1 /gene="CLDN12" /replace="g" /replace="t" /db_xref="dbSNP:2115852648" variation 4..6 /gene="CLDN12" /replace="aac" /replace="aacaac" /db_xref="dbSNP:1796774149" variation 6 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:765746790" variation 7 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796774304" variation 8 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:1796774373" variation 9 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:896219909" variation 10 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:1796774534" variation 12 /gene="CLDN12" /replace="a" /replace="t" /db_xref="dbSNP:1796774614" variation 15 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1796774687" variation 17 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:370765493" variation 18 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1222423857" variation 20 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1011927155" variation 21 /gene="CLDN12" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:751279674" variation 22 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:1385384287" variation 24 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796775480" variation 25 /gene="CLDN12" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1398100775" variation 29 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796775676" variation 30..33 /gene="CLDN12" /replace="gaga" /replace="gagagaga" /db_xref="dbSNP:1407169883" variation 30 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796775754" variation 32 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796775914" variation 34 /gene="CLDN12" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:143733597" variation 35 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:1425856010" variation 36 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1168508452" variation 38 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:1796776262" variation 39 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:2115852942" variation 40 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1475702583" variation 42 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:980932371" variation 44 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:1190789610" variation 45 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796776471" variation 47 /gene="CLDN12" /replace="g" /replace="t" /db_xref="dbSNP:1227182688" variation 48 /gene="CLDN12" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1272088946" variation 49 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1459639556" variation 50 /gene="CLDN12" /replace="a" /replace="t" /db_xref="dbSNP:1796776658" variation 53 /gene="CLDN12" /replace="g" /replace="t" /db_xref="dbSNP:926736878" variation 57 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:544870413" variation 61 /gene="CLDN12" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1195806368" variation 63 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:2115853113" variation 65 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1322992370" variation 66 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796776863" variation 70 /gene="CLDN12" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:552258236" variation 71 /gene="CLDN12" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1247490960" variation 73 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1796777009" variation 76 /gene="CLDN12" /replace="a" /replace="c" /db_xref="dbSNP:931405359" variation 77 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796777129" variation 78 /gene="CLDN12" /replace="t" /replace="tt" /db_xref="dbSNP:1796777188" variation 80 /gene="CLDN12" /replace="a" /replace="t" /db_xref="dbSNP:1264722319" variation 81 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1450737590" variation 84 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796777328" variation 85 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796777380" variation 86 /gene="CLDN12" /replace="g" /replace="t" /db_xref="dbSNP:1796777438" variation 87 /gene="CLDN12" /replace="a" /replace="c" /db_xref="dbSNP:1048901650" variation 88 /gene="CLDN12" /replace="a" /replace="t" /db_xref="dbSNP:1796777552" exon 90..179 /gene="CLDN12" /inference="alignment:Splign:2.1.0" variation 91 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1248400932" variation 93 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1796817645" variation 95 /gene="CLDN12" /replace="g" /replace="t" /db_xref="dbSNP:963982658" variation 98 /gene="CLDN12" /replace="a" /replace="t" /db_xref="dbSNP:1796817809" variation 104 /gene="CLDN12" /replace="a" /replace="t" /db_xref="dbSNP:972278194" variation 106 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:116804658" variation 107 /gene="CLDN12" /replace="g" /replace="t" /db_xref="dbSNP:1796818109" variation 108 /gene="CLDN12" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1368552758" variation 109..111 /gene="CLDN12" /replace="t" /replace="tgt" /db_xref="dbSNP:773152966" variation 110 /gene="CLDN12" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:954322006" variation 124 /gene="CLDN12" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:987257325" variation 125 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:910285876" variation 130 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:2115863292" variation 133..134 /gene="CLDN12" /replace="t" /replace="tt" /db_xref="dbSNP:1796818542" variation 133 /gene="CLDN12" /replace="g" /replace="t" /db_xref="dbSNP:1796818489" variation 135 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:1206373165" variation 139 /gene="CLDN12" /replace="" /replace="g" /db_xref="dbSNP:1796818649" variation 141 /gene="CLDN12" /replace="a" /replace="t" /db_xref="dbSNP:1796818701" variation 148 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:911440597" variation 149 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:755004916" variation 151 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1796818776" variation 153 /gene="CLDN12" /replace="a" /replace="t" /db_xref="dbSNP:551241265" variation 162 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1372481614" variation 165 /gene="CLDN12" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1430548490" variation 168 /gene="CLDN12" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1357263224" variation 169 /gene="CLDN12" /replace="g" /replace="t" /db_xref="dbSNP:781426929" variation 170 /gene="CLDN12" /replace="a" /replace="aa" /db_xref="dbSNP:1796819264" variation 171 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:925780228" variation 172 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1242659231" variation 174 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:185475099" variation 178 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1394975547" variation 179 /gene="CLDN12" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:934587691" exon 180..3490 /gene="CLDN12" /inference="alignment:Splign:2.1.0" misc_feature 186..188 /gene="CLDN12" /note="upstream in-frame stop codon" variation 188 /gene="CLDN12" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:942749126" variation 189 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:777642503" variation 191 /gene="CLDN12" /replace="a" /replace="g" /db_xref="dbSNP:1796990526" variation 192 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:2115896242" variation 193 /gene="CLDN12" /replace="a" /replace="c" /db_xref="dbSNP:1584668248" variation 196 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:914599269" variation 199 /gene="CLDN12" /replace="c" /replace="g" /db_xref="dbSNP:1329882679" variation 203 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1210708993" variation 206 /gene="CLDN12" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:946000977" variation 209 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:749239357" variation 211 /gene="CLDN12" /replace="c" /replace="t" /db_xref="dbSNP:1796990980" CDS 213..947 /gene="CLDN12" /codon_start=1 /product="claudin-12" /protein_id="NP_036261.1" /db_xref="CCDS:CCDS5618.1" /db_xref="GeneID:9069" /db_xref="HGNC:HGNC:2034" /db_xref="MIM:611232" /translation="
MGCRDVHAATVLSFLCGIASVAGLFAGTLLPNWRKLRLITFNRNEKNLTVYTGLWVKCARYDGSSDCLMYDTTWYSSVDQLDLRVLQFALPLSMLIAMGALLLCLIGMCNTAFRSSVPNIKLAKCLVNSAGCHLVAGLLFFLAGTVSLSPSIWVIFYNIHLNKKFEPVFSFDYAVYVTIASAGGLFMTSLILFIWYCTCKSLPSPFWQPLYSHPPSMHTYSQPYSARSRLSAIEIDIPVVSHTT"
misc_feature 243..305
/gene="CLDN12"
/note="propagated from UniProtKB/Swiss-Prot (P56749.1);
transmembrane region"
misc_feature 474..536
/gene="CLDN12"
/note="propagated from UniProtKB/Swiss-Prot (P56749.1);
transmembrane region"
misc_feature 618..680
/gene="CLDN12"
/note="propagated from UniProtKB/Swiss-Prot (P56749.1);
transmembrane region"
misc_feature 735..797
/gene="CLDN12"
/note="propagated from UniProtKB/Swiss-Prot (P56749.1);
transmembrane region"
misc_feature 894..896
/gene="CLDN12"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (P56749.1); phosphorylation site"
misc_feature 903..905
/gene="CLDN12"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:19690332,
ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (P56749.1); phosphorylation site"
variation 213
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1341616884"
variation 220
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1796991072"
variation 221
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:757087056"
variation 222
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1796991212"
variation 223
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:200372770"
variation 224
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201163165"
variation 226
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1796991447"
variation 228
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:745619799"
variation 230
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1796991550"
variation 233
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1180615075"
variation 234
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:761164855"
variation 241
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:775261538"
variation 246
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1796991783"
variation 250
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115896574"
variation 251
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:746541829"
variation 255
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:902429408"
variation 256
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:768207460"
variation 265
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1796991990"
variation 266
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:374340236"
variation 269
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:762394956"
variation 285
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1796992187"
variation 293
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:765595005"
variation 296
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1796992247"
variation 300
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:563004910"
variation 305
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:763251187"
variation 306
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:766633842"
variation 307
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1230245825"
variation 308
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1796992501"
variation 317
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1356210861"
variation 320
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1796992608"
variation 321
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056206386"
variation 322
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:894925508"
variation 327
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:530429481"
variation 328
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:755075227"
variation 329
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1421096252"
variation 331
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115896933"
variation 335
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:767652846"
variation 340
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:752656827"
variation 344
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:140108357"
variation 345
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1252002472"
variation 346..352
/gene="CLDN12"
/replace="agaa"
/replace="agaagaa"
/db_xref="dbSNP:1796993185"
variation 350
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1796993244"
variation 354
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1388876915"
variation 358
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1185916821"
variation 362
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:778948294"
variation 365
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1257994346"
variation 366
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1445655137"
variation 369
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1796993920"
variation 371
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:745707657"
variation 374
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:758236906"
variation 376
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208351338"
variation 377
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433317264"
variation 381
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:779918948"
variation 383
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017072069"
variation 384
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461239450"
variation 387
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1308429047"
variation 390
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:367561054"
variation 391
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1796994585"
variation 394
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:371660301"
variation 398
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:17862175"
variation 399
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:200164858"
variation 401
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1562969445"
variation 404
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:970838406"
variation 411..418
/gene="CLDN12"
/replace=""
/replace="tgcctgat"
/db_xref="dbSNP:761720130"
variation 415..433
/gene="CLDN12"
/replace="tg"
/replace="tgatgtacgacactacttg"
/db_xref="dbSNP:1796995132"
variation 421..425
/gene="CLDN12"
/replace="ac"
/replace="acgac"
/db_xref="dbSNP:1303999268"
variation 422
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:185427290"
variation 423
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:368401578"
variation 426
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1796995439"
variation 428..438
/gene="CLDN12"
/replace="tact"
/replace="tacttggtact"
/db_xref="dbSNP:1796995497"
variation 429
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1275779056"
variation 430
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1445448312"
variation 434..435
/gene="CLDN12"
/replace=""
/replace="ccc"
/db_xref="dbSNP:1796995702"
variation 436
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1484264687"
variation 437
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1219772042"
variation 438
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:763344432"
variation 439
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:372373015"
variation 440
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1488499672"
variation 443
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:200281270"
variation 444
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:774643531"
variation 452
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:759812081"
variation 453
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1796996253"
variation 455
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:767596396"
variation 457
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1584668526"
variation 461
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:926814363"
variation 462
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422564484"
variation 463
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:756709778"
variation 465
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:964186372"
variation 467
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:868742300"
variation 470
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1796996690"
variation 479
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1349545698"
variation 482
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1471326978"
variation 492
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1233688018"
variation 494
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:566157753"
variation 497
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1796997046"
variation 500
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:539978988"
variation 501
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:750382986"
variation 503
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:990256012"
variation 504
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:76988207"
variation 505
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:780008661"
variation 506
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1584668597"
variation 508
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1244278168"
variation 510
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1360064110"
variation 515
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1796997647"
variation 517
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1796997721"
variation 518
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751243867"
variation 521
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1796997877"
variation 522
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:754688920"
variation 527
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:79632494"
variation 529
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1239862137"
variation 530
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1796998129"
variation 538
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1485280228"
variation 539
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1189107272"
variation 540
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1249840221"
variation 546
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442500935"
variation 547
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1162698211"
variation 553
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1796998536"
variation 559
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:747740249"
variation 560
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:34378679"
variation 561
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:749812448"
variation 568
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:370065476"
variation 569
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:373294317"
variation 572..583
/gene="CLDN12"
/replace="caaactggccaa"
/replace="caaactggccaaactggccaa"
/db_xref="dbSNP:771967868"
variation 574
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1796999322"
variation 577
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:146056566"
variation 580
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409135371"
variation 581
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1321764678"
variation 583
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367983663"
variation 587
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450838716"
variation 590
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471726358"
variation 591
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:555785316"
variation 594
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:759773648"
variation 595
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:772387218"
variation 598
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1281762078"
variation 599
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797000329"
variation 603
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797000393"
variation 611
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1315755536"
variation 612
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1208839238"
variation 617..618
/gene="CLDN12"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:911772551"
variation 619
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775546156"
variation 623
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1200239537"
variation 626
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:760904190"
variation 629
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1182972744"
variation 630
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1237832831"
variation 631
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1421803319"
variation 641
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:890079426"
variation 644
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1183769329"
variation 648
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1406103443"
variation 658
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456713791"
variation 659
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:764256390"
variation 660
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753910760"
variation 661
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762986952"
variation 662
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:766378731"
variation 664
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:751390117"
variation 666
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1227469450"
variation 673
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797002010"
variation 674
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:754704274"
variation 676
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:774617903"
variation 677
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1008641536"
variation 682
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1349496355"
variation 683
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1228407374"
variation 685
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:139669349"
variation 686
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115899093"
variation 690
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1284739711"
variation 693
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797002541"
variation 698
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1562969631"
variation 699..704
/gene="CLDN12"
/replace="aag"
/replace="aagaag"
/db_xref="dbSNP:773058903"
variation 700
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1320879422"
variation 703
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:752284824"
variation 708
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:761520976"
variation 710
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:755709686"
variation 715
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:777274351"
variation 717
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797003096"
variation 725
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1366238040"
variation 730
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:748759222"
variation 733
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797003265"
variation 737
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797003319"
variation 743
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797003409"
variation 747
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:993873530"
variation 748
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1346219704"
variation 753
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:757786645"
variation 754
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:779267034"
variation 755
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:746285653"
variation 756
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1479528196"
variation 759
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115899421"
variation 760
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797003916"
variation 763
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797003989"
variation 764
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:574014370"
variation 765
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:149798695"
variation 767
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1416451842"
variation 772
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797004322"
variation 775
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:2115899527"
variation 776
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:747247531"
variation 779
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797004444"
variation 785
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797004504"
variation 788
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:779705246"
variation 791
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:768932001"
variation 794
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:776879207"
variation 804
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:761934562"
variation 806
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:148668482"
variation 807
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1191786166"
variation 809
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:759438469"
variation 810
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797005046"
variation 812
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:142157384"
variation 814
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:767199576"
variation 815
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:955988159"
variation 818
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1375782905"
variation 825
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:752426881"
variation 826
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1486801818"
variation 829
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1584668952"
variation 830
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797005569"
variation 833
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:755799542"
variation 834
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:763690839"
variation 836
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:753398499"
variation 839
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1206115664"
variation 840
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:756729926"
variation 841
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:779542822"
variation 842
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1198251095"
variation 845
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008503268"
variation 847..849
/gene="CLDN12"
/replace="ccc"
/replace="ccccc"
/db_xref="dbSNP:1223711404"
variation 848
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:746347780"
variation 851
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1166728057"
variation 852
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1389906667"
variation 853
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:758882760"
variation 854
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797006493"
variation 855
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1170053675"
variation 857
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:780285790"
variation 858
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797006667"
variation 859
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:376598671"
variation 861
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:747335564"
variation 862
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797006893"
variation 863
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1332390514"
variation 864
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:970708263"
variation 866
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1428520245"
variation 869
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797007228"
variation 871..876
/gene="CLDN12"
/replace="ac"
/replace="actcac"
/db_xref="dbSNP:760654070"
variation 872
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:769020005"
variation 874
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797007490"
variation 875
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1230381453"
variation 879
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:189780617"
variation 881
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748275826"
variation 883
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:769754148"
variation 886
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1268142593"
variation 888
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:147857522"
variation 890
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:759400199"
variation 891
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:141430153"
variation 892
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:865961955"
variation 893
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:775287956"
variation 895
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760443285"
variation 897
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:747014345"
variation 898
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:763777074"
variation 900
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429133550"
variation 906
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756850579"
variation 909
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1398470804"
variation 911
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1187804658"
variation 912
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:764668076"
variation 913
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:749880828"
variation 919
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:967846329"
variation 921
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1271494883"
variation 922
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1436940870"
variation 923
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:758860405"
variation 926
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:780560088"
variation 938
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:752018635"
variation 939
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797010396"
variation 941
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1266312378"
variation 948
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1562969817"
variation 949..952
/gene="CLDN12"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:977418221"
variation 951
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:928650226"
variation 952
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:2115900827"
variation 955
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:374720515"
variation 956
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1206908768"
variation 958
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1267989651"
variation 965
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1465732406"
variation 967..1063
/gene="CLDN12"
/replace=""
/replace="taaagaaaacttcttgtagcctcacattccccttgtgcaaagagctct
tttggacctacatacattttcctttgtttttgaccaatcaatgaagcca"
/db_xref="dbSNP:1797011251"
variation 970
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:375989620"
variation 971
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797011398"
variation 977
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:769996911"
variation 979
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:182726869"
variation 981
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797011748"
variation 982
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1187748511"
variation 986..987
/gene="CLDN12"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1226803013"
variation 987
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:147269114"
variation 988
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316158945"
variation 995
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:866289679"
variation 996
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1584669245"
variation 997
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395737979"
variation 1000
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797013768"
variation 1002
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1377257671"
variation 1003
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797013910"
variation 1005
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:900273326"
variation 1008
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797014053"
variation 1017
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1179310503"
variation 1019
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:947945946"
variation 1021
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797014312"
variation 1023
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:999866390"
variation 1025
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:898274718"
variation 1026
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797014547"
variation 1027
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797014627"
variation 1029
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:140861444"
variation 1030
/gene="CLDN12"
/replace=""
/replace="a"
/db_xref="dbSNP:1797014858"
variation 1030
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:891619549"
variation 1046
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115901329"
variation 1047
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1427727674"
variation 1048
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797015010"
variation 1050
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1386933821"
variation 1052
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1188004664"
variation 1054..1059
/gene="CLDN12"
/replace="aa"
/replace="aatgaa"
/db_xref="dbSNP:2115901396"
variation 1055
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:532905007"
variation 1056
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:890800093"
variation 1057
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1178538518"
variation 1071
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1483121516"
variation 1078
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1584669303"
variation 1079
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:3810874"
variation 1081
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1414265200"
variation 1086
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:187870115"
variation 1092
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797015989"
variation 1095
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:560572122"
variation 1096
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1331745815"
variation 1097
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797016195"
variation 1099
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1272440914"
variation 1104
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:906557611"
variation 1110
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1244540414"
variation 1112..1123
/gene="CLDN12"
/replace="tatatta"
/replace="tatattatatta"
/db_xref="dbSNP:1797016509"
variation 1114
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115901668"
variation 1119
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1378691088"
variation 1123
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797016620"
variation 1127
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1447132010"
variation 1137
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:774645854"
variation 1138
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1033653763"
variation 1141
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:959452294"
variation 1145
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797016909"
variation 1150
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797016968"
variation 1151
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:973856566"
variation 1153
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1562969901"
variation 1154
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:900083050"
variation 1156
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306254029"
variation 1157
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1236327058"
variation 1158
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:2115901874"
variation 1159
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797017290"
variation 1161
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1011768718"
variation 1169
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163722599"
variation 1171..1172
/gene="CLDN12"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1797017629"
variation 1171
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1256518254"
variation 1172
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797017692"
variation 1173
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797017748"
variation 1176
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1027862498"
variation 1177
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1473129326"
variation 1179
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797017943"
variation 1180
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797017993"
variation 1183
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1251638835"
variation 1189
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1180638747"
variation 1198
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797018142"
variation 1200..1201
/gene="CLDN12"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1797018186"
variation 1201
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1490998943"
variation 1205
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1267404539"
variation 1206
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1343977226"
variation 1212
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:191882778"
variation 1214
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797018457"
variation 1217
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:967541357"
variation 1223
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797018614"
variation 1224
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:547780944"
variation 1231
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797018812"
variation 1234
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:2115902195"
variation 1240
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797018888"
variation 1243..1291
/gene="CLDN12"
/replace="catgttaaagaatgatggttagcagaagctgttgtatacaatcttcat
g"
/replace="catgttaaagaatgatggttagcagaagctgttgtatacaatcttcat
gttaaagaatgatggttagcagaagctgttgtatacaatcttcatg"
/db_xref="dbSNP:1797018963"
variation 1244
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1198534959"
variation 1245
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:759662047"
variation 1249
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:2115902237"
variation 1251
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:559947062"
variation 1254
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797019216"
variation 1257
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797019297"
variation 1258
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797019376"
variation 1262
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:983742931"
variation 1265
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115902293"
variation 1273
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:998912183"
variation 1275
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1328221542"
variation 1277
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797019659"
variation 1279
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797019714"
variation 1280
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1459234257"
variation 1281
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:912147725"
variation 1283
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:533404402"
variation 1295
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797020021"
variation 1296..1298
/gene="CLDN12"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1797020107"
variation 1301
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1584669443"
variation 1303
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115902441"
variation 1305
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:944930760"
variation 1306
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797020354"
variation 1307
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1035697540"
variation 1308..1312
/gene="CLDN12"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1341622967"
variation 1313
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1324237708"
variation 1318
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:183250663"
variation 1321
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201561756"
variation 1323
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:921560776"
variation 1324
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:17865130"
variation 1327
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797021149"
variation 1328
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:775800641"
variation 1330
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1171166572"
variation 1332
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:916540737"
variation 1334
/gene="CLDN12"
/replace=""
/replace="c"
/db_xref="dbSNP:1411668520"
variation 1334
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402960380"
variation 1335
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797021627"
variation 1338
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797021699"
variation 1340
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:761220112"
variation 1360
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797021861"
variation 1367
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:969698079"
variation 1368
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378745647"
variation 1370
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465816431"
variation 1373
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1449383814"
variation 1377
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797022284"
variation 1380
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1263307715"
variation 1382
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208952414"
variation 1388
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:973988290"
variation 1402
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:2115902887"
variation 1404
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017104"
variation 1406
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:891653604"
variation 1409
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1345566892"
variation 1417
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797022778"
variation 1420
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274194047"
variation 1422
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797022886"
variation 1425
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797022933"
variation 1426..1429
/gene="CLDN12"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:1232533722"
variation 1430
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1329410221"
variation 1432
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115903074"
variation 1433
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:945853582"
variation 1435
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:549473969"
variation 1436
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:533121034"
variation 1438
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:760268284"
variation 1439
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1330426305"
variation 1446
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471169901"
variation 1448
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1231028407"
variation 1450
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797023526"
variation 1455
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797023593"
variation 1456
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:567681750"
variation 1464
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115903256"
variation 1466
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1172501538"
variation 1471
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1477360361"
variation 1478
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374271262"
variation 1480
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797023880"
variation 1481
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1188685236"
variation 1484
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797023965"
variation 1493
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:550000862"
variation 1499
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797024060"
variation 1503
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318404977"
variation 1504
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1651805770"
variation 1505
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1336291604"
variation 1506
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797024205"
variation 1509
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1562970064"
variation 1510
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:2115903425"
variation 1515
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1245839054"
variation 1520
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1205265446"
variation 1523
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442790804"
variation 1526
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1017105"
variation 1527
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1012253900"
variation 1528
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797024663"
variation 1529
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797024716"
variation 1536
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1017106"
variation 1538
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:895147073"
variation 1541
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797024838"
variation 1542
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797024924"
variation 1543..1551
/gene="CLDN12"
/replace="aga"
/replace="agaataaga"
/db_xref="dbSNP:552639099"
variation 1544
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797025017"
variation 1548
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797025067"
variation 1555
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1295686881"
variation 1560
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1268208384"
variation 1564
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797025225"
variation 1577
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:994966682"
variation 1586..1587
/gene="CLDN12"
/replace=""
/replace="at"
/db_xref="dbSNP:903352549"
variation 1586
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:2115903714"
variation 1591
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1413233891"
variation 1592
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797025472"
variation 1596
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797025521"
variation 1601
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797025594"
variation 1605
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1399297577"
variation 1606
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:374000239"
variation 1609
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115903807"
variation 1610
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797025797"
variation 1612
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1428553214"
variation 1615
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451510157"
variation 1618
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1584669652"
variation 1624
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1028134579"
variation 1627
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1387862871"
variation 1633
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115903888"
variation 1640
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797026258"
variation 1646
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797026336"
variation 1648
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1185042417"
variation 1651
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1472953732"
variation 1654
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1236655377"
variation 1655
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797026622"
variation 1664
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797026687"
variation 1665
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:950806358"
variation 1671
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797026821"
variation 1681
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797028208"
variation 1682
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115904009"
variation 1684..1689
/gene="CLDN12"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1562970120"
variation 1688
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:984038424"
variation 1690
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797028421"
variation 1694
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797028511"
variation 1696
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1439444036"
variation 1697
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1275284469"
variation 1700
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797028756"
variation 1705
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:998944770"
variation 1710
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797028929"
variation 1712
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797028992"
variation 1714
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797029074"
variation 1716
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1019037247"
variation 1717
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:966267349"
variation 1724
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1478353974"
variation 1726
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797029420"
variation 1728
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797029491"
variation 1735
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797029560"
variation 1738
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1283932650"
variation 1739
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1446308788"
variation 1745
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1480633045"
variation 1752
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1584669723"
variation 1755
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797029921"
variation 1757
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797029989"
variation 1761
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584669725"
variation 1763
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:376739855"
variation 1764
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1584669740"
variation 1766
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:567106439"
variation 1778..1782
/gene="CLDN12"
/replace="tct"
/replace="tctct"
/db_xref="dbSNP:1409819331"
variation 1779
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1584669759"
variation 1781
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:534834365"
variation 1788
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:754923918"
variation 1790
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797030748"
variation 1791
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368142857"
variation 1798
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:963389194"
variation 1802
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1421044873"
variation 1803
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:974400768"
variation 1806
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:974961464"
variation 1811
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:921635723"
variation 1814
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797031478"
variation 1822
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:935650705"
variation 1823
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797031637"
variation 1824
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1471043531"
variation 1826
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797031714"
variation 1828
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797031786"
variation 1830
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1293571453"
variation 1832
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1252356341"
variation 1836
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:750152497"
variation 1840..1842
/gene="CLDN12"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1384990512"
variation 1845
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1249674258"
variation 1849
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797032334"
variation 1850
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:912992887"
variation 1850
/gene="CLDN12"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1797032473"
variation 1857
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:982612622"
variation 1864
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797032618"
variation 1868
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1289445533"
variation 1870
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1226894064"
variation 1873
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1331653911"
variation 1874..1875
/gene="CLDN12"
/replace="a"
/replace="aa"
/db_xref="dbSNP:140787647"
variation 1880
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1217821009"
variation 1881
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1349222438"
variation 1883
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:945789489"
variation 1888
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797033299"
variation 1892
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797033352"
variation 1893
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1436593969"
variation 1894
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1348873072"
variation 1896..1897
/gene="CLDN12"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1321175332"
variation 1898..1924
/gene="CLDN12"
/replace="ccttgattcatt"
/replace="ccttgattcattcacccttgattcatt"
/db_xref="dbSNP:932326055"
variation 1898
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797033649"
variation 1899
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:193147106"
variation 1906
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1584669868"
variation 1907
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1158199722"
variation 1911
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1247314127"
variation 1912
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471546613"
variation 1921
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:906996301"
variation 1928
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:920946811"
variation 1929
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:937281533"
variation 1930..1934
/gene="CLDN12"
/replace="cccc"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:947032141"
variation 1930
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1466456646"
variation 1931
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:778741633"
variation 1932
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:895178364"
variation 1933
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797034687"
variation 1934
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:995263893"
variation 1935
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797034822"
variation 1936
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797034880"
variation 1941
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1049027514"
variation 1942
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797035028"
variation 1949
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1266011398"
variation 1950
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:903426027"
variation 1952
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193362122"
variation 1957..1962
/gene="CLDN12"
/replace="atatat"
/replace="atatatat"
/db_xref="dbSNP:1261530209"
variation 1957
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:886530167"
variation 1959
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:934869590"
variation 1960
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1057210209"
variation 1963
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1436790996"
variation 1971
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:547044063"
variation 1978
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:571569072"
variation 1980
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1019108615"
variation 1983
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797035643"
variation 1987
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:556714945"
variation 1988
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115905351"
variation 1989
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797035747"
variation 1990
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1455939440"
variation 1997
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:996411871"
variation 2000
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:575067068"
variation 2001
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1029180653"
variation 2005
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:538983399"
variation 2007
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:957622732"
variation 2009
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797036301"
variation 2019
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797036351"
variation 2021
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115905499"
variation 2024
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797036400"
variation 2026
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424520538"
variation 2028
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797036501"
variation 2033
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:899170131"
variation 2036
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451513203"
variation 2038
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797036674"
variation 2042
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:754778051"
variation 2045
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1361115269"
variation 2050
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797036824"
variation 2057
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797036877"
variation 2058
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797036932"
variation 2060
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797036982"
variation 2062..2078
/gene="CLDN12"
/replace="a"
/replace="acctggcagttggggaa"
/db_xref="dbSNP:1399382784"
variation 2071
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797037077"
variation 2073
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1188257270"
variation 2074
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1463822025"
variation 2075
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797037228"
variation 2076
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797037279"
variation 2087
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:142246998"
variation 2090
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1027358393"
variation 2091
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:11563542"
variation 2092
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1230005617"
variation 2102
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797037616"
variation 2103
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748038842"
variation 2112
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1296423810"
variation 2113
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432532566"
variation 2115
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797037885"
variation 2117
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:928487682"
variation 2119
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:572751121"
variation 2121
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1465452920"
variation 2123
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:975568982"
variation 2128
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:576056629"
variation 2130
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797038407"
variation 2133
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:2115905908"
variation 2135
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1321153174"
variation 2137
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1168187142"
variation 2138..2139
/gene="CLDN12"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1427013136"
variation 2138
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584670066"
variation 2140
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1243896507"
variation 2146
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1258669180"
variation 2147
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:947073657"
variation 2149
/gene="CLDN12"
/replace=""
/replace="c"
/db_xref="dbSNP:1797039089"
variation 2149
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1483181859"
variation 2151
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797039174"
variation 2163
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1256038868"
variation 2167
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797039308"
variation 2168
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797039388"
variation 2170
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797039454"
variation 2173
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1206594484"
variation 2174
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584670098"
variation 2182
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:540218408"
variation 2184
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1273357484"
variation 2185
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288305075"
variation 2186
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797039917"
variation 2189
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:536938497"
variation 2193
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:151249770"
variation 2194
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:934927186"
variation 2196
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797040238"
variation 2197
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:2115906196"
variation 2199
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:555238649"
variation 2202
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797040431"
variation 2204
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1376806671"
variation 2208
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797040563"
variation 2210
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:895991227"
variation 2215
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:948855688"
variation 2218..2224
/gene="CLDN12"
/replace="ca"
/replace="cagtcca"
/db_xref="dbSNP:1044911159"
variation 2219
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1049534377"
variation 2220
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:886436147"
variation 2223
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1168084725"
variation 2226
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797041120"
variation 2227
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1182013421"
variation 2229
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370441770"
variation 2231
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1562970326"
variation 2233
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1255085510"
variation 2242
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1005408928"
variation 2245
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1165859003"
variation 2257
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584670166"
variation 2258
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423601634"
variation 2265
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797041609"
variation 2269
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1562970332"
variation 2270
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797041698"
variation 2271
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:772162884"
variation 2276
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1040420941"
variation 2280
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1483696092"
variation 2282
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797041912"
variation 2283
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115906514"
variation 2285
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:533659745"
variation 2287
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797042009"
variation 2289
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:781394155"
variation 2294
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1489227199"
variation 2302
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:996320503"
variation 2305
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1421494035"
variation 2307
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797042249"
variation 2308
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:775641475"
variation 2309
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:899246704"
variation 2312
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797042455"
variation 2313
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797042500"
variation 2318
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115906685"
variation 2322
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:995272217"
variation 2331
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797042607"
variation 2336
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1290038988"
variation 2342
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797042707"
variation 2345
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1179948472"
variation 2352
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1380422565"
variation 2354
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026303981"
variation 2356
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:747407397"
variation 2360
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1584670238"
variation 2366
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1029090662"
variation 2370
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:17861306"
variation 2372
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:886408648"
variation 2374..2376
/gene="CLDN12"
/replace="t"
/replace="tct"
/db_xref="dbSNP:1797043169"
variation 2381
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1004148918"
variation 2384
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:34833025"
variation 2389
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584670253"
variation 2394
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1019502395"
variation 2399
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1294333584"
variation 2402
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1457646450"
variation 2403
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:2115906955"
variation 2405
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797043495"
variation 2409
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:957866681"
variation 2413
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1360627967"
variation 2414
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:965213810"
variation 2417
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1011794834"
variation 2425
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:745904312"
variation 2434
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:552033731"
variation 2436..2437
/gene="CLDN12"
/replace=""
/replace="tctttagccttat"
/db_xref="dbSNP:1797043926"
variation 2436
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797043882"
variation 2438
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1020409995"
variation 2439
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797044070"
variation 2440
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:758483645"
variation 2441
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1178971100"
variation 2451
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1434396237"
variation 2454
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1267511875"
variation 2465
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:967063239"
variation 2474
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208852565"
variation 2481
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797044582"
variation 2483
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797044640"
variation 2484
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797044697"
variation 2485
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:769881194"
variation 2486
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797044787"
variation 2487
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1378687437"
variation 2488
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1562970407"
variation 2491
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797044921"
variation 2495
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1269744016"
variation 2497
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797045019"
variation 2503
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1209145387"
variation 2506
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1328320779"
variation 2507
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450772647"
variation 2513
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:563896573"
variation 2514
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:531095413"
variation 2525
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386395021"
variation 2527
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797045442"
variation 2534
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584670348"
variation 2542
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797045540"
variation 2545
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:17867644"
variation 2552..2557
/gene="CLDN12"
/replace="ag"
/replace="agctag"
/db_xref="dbSNP:1797045671"
variation 2553
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797045730"
variation 2556
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:928352216"
variation 2561
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458105363"
variation 2563
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:978863706"
variation 2571
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:762216364"
variation 2574
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1715026992"
variation 2577
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1468077747"
variation 2579
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:924298842"
variation 2583
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797046266"
variation 2586
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797046336"
variation 2589
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797046394"
variation 2591
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:934288696"
variation 2599
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797046575"
variation 2601
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:991328066"
variation 2608
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1452131616"
variation 2612
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1249523650"
variation 2618
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797046858"
variation 2620
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797046932"
variation 2621
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1188892883"
variation 2623..2642
/gene="CLDN12"
/replace=""
/replace="tgtatttggtactttttccc"
/db_xref="dbSNP:1464268800"
variation 2623
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797047096"
variation 2624
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:919730924"
variation 2625
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:931262369"
variation 2631
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1211293525"
variation 2632
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797047354"
variation 2640
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:764872441"
variation 2641
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1202086053"
variation 2650
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:540782667"
variation 2651
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:907894060"
variation 2655
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:940676159"
variation 2657
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797047650"
variation 2658
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1256619712"
variation 2661..2670
/gene="CLDN12"
/replace="tata"
/replace="tatatatata"
/replace="tatatatatata"
/db_xref="dbSNP:1233683720"
variation 2662
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1300096104"
variation 2664
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1040328332"
variation 2666
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:901949934"
variation 2667
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:917492584"
variation 2669
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797048071"
variation 2672
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:932036114"
variation 2673
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:559357320"
variation 2677..2679
/gene="CLDN12"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1797048243"
variation 2683
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403567804"
variation 2684
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:893301629"
variation 2689
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797048395"
variation 2691
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:766157192"
variation 2695
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1171425269"
variation 2696
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797048523"
variation 2704
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:534758357"
variation 2705
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:777199816"
variation 2706
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:930760045"
variation 2709..2713
/gene="CLDN12"
/replace="ag"
/replace="agtag"
/db_xref="dbSNP:1047817247"
variation 2714
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:886441156"
variation 2717
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1448550405"
variation 2719
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1240112127"
variation 2722
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1189399121"
variation 2724
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:902873098"
variation 2726
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1002551520"
variation 2729
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584670467"
variation 2730
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1442880662"
variation 2731
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797049566"
variation 2732
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1255396559"
variation 2733..2739
/gene="CLDN12"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:1562970505"
variation 2734
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1176630485"
variation 2738
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1035319829"
variation 2739
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1008866447"
variation 2740
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:958446477"
variation 2741
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797050127"
variation 2743
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:546965228"
variation 2748
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1027265526"
variation 2749
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797050282"
variation 2754
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797050326"
variation 2757
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1175047169"
variation 2765
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1584670514"
variation 2766
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:952560771"
variation 2773
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:571487034"
variation 2776
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1468418122"
variation 2779
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:397759219"
variation 2780
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:397829267"
variation 2781
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1333632831"
variation 2786
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797050729"
variation 2790
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797050768"
variation 2791
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1584670545"
variation 2792
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797050880"
variation 2793
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1401034875"
variation 2800
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1268738832"
variation 2803
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:901086369"
variation 2805
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797051063"
variation 2806
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1341525427"
variation 2808
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:2115908811"
variation 2809
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:577566452"
variation 2811
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1312801622"
variation 2812
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797051232"
variation 2814
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797051282"
variation 2815
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446170006"
variation 2821
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:184613376"
variation 2822
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:943930679"
variation 2823
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:769109092"
variation 2826
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:751187006"
variation 2829
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1164716133"
variation 2839
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797051611"
variation 2840
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:932109832"
variation 2851
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:999951759"
variation 2852..2855
/gene="CLDN12"
/replace=""
/replace="tttt"
/db_xref="dbSNP:1370335953"
variation 2857
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1050526265"
variation 2858
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797051819"
variation 2859
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797051879"
variation 2864
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1048883"
variation 2866
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797052050"
variation 2874
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:893323586"
variation 2876
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797052208"
variation 2878
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301013251"
variation 2879
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1031349699"
variation 2883
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797052448"
variation 2887
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:770889312"
variation 2890
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1042255724"
variation 2899
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797052620"
variation 2901
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797052671"
variation 2910
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:556800887"
variation 2913
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1205988867"
variation 2918
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797052814"
variation 2924
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1437404656"
variation 2927
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1220031653"
variation 2930
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797052954"
variation 2931
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:754831345"
variation 2936..2937
/gene="CLDN12"
/replace=""
/replace="tata"
/db_xref="dbSNP:1797053046"
variation 2938
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:992452555"
variation 2940
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258313188"
variation 2941
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797053172"
variation 2952
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:767405026"
variation 2953
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:774762433"
variation 2961
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797053359"
variation 2966
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:970325178"
variation 2967
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115909450"
variation 2968
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1035394292"
variation 2974
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797053515"
variation 2975
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352898945"
variation 2976
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584670657"
variation 2980
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:2115909510"
variation 2981
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797053669"
variation 2982..2987
/gene="CLDN12"
/replace="ag"
/replace="agacag"
/db_xref="dbSNP:1288375953"
variation 2982
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797053723"
variation 2983
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797053824"
variation 2985
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:894138443"
variation 2988..2994
/gene="CLDN12"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:1797053927"
variation 2994
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:781641197"
variation 2997
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797054028"
variation 3000
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797054079"
variation 3003
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1247987207"
variation 3009
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1012698606"
variation 3013
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:568718729"
variation 3014..3021
/gene="CLDN12"
/replace="at"
/replace="ataaacat"
/db_xref="dbSNP:1797054344"
variation 3014
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797054298"
variation 3015
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797054403"
variation 3018
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026715065"
variation 3023
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797054515"
variation 3024
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115909795"
variation 3025
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1352335014"
variation 3032
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:186714887"
variation 3033
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1405647009"
variation 3034
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:982647638"
variation 3038
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1478681950"
variation 3040
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1162570148"
variation 3041
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797054998"
variation 3044
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:558116406"
variation 3047
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:572884216"
variation 3057
/gene="CLDN12"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:930764716"
variation 3060
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:191175070"
variation 3072
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797055506"
variation 3078
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1182906250"
variation 3081
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1469690049"
variation 3083
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797055664"
variation 3085
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:370567033"
variation 3088
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1465346932"
variation 3092
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1224019264"
variation 3095
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797055868"
variation 3096
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797055922"
variation 3103
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:976635967"
variation 3104
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115910133"
variation 3106
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797056014"
variation 3110..3114
/gene="CLDN12"
/replace="tt"
/replace="ttatt"
/db_xref="dbSNP:1797056080"
variation 3111
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:923308201"
variation 3112
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:755973015"
variation 3113
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1047849387"
variation 3116
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:745517196"
variation 3117
/gene="CLDN12"
/replace=""
/replace="c"
/db_xref="dbSNP:1797056453"
variation 3119
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797056532"
variation 3120..3127
/gene="CLDN12"
/replace="ttt"
/replace="ttttcttt"
/db_xref="dbSNP:1272900117"
variation 3127
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:931973835"
variation 3128
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797056743"
variation 3129
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331761043"
variation 3131
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1293475661"
variation 3141
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:986645515"
variation 3142
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797056958"
variation 3145
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:544649141"
variation 3146
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797057066"
variation 3153
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797057140"
variation 3155
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:2115910364"
variation 3163
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:947424244"
variation 3164
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1289526240"
variation 3166
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1041890726"
variation 3167
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:9731"
variation 3168
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1695614681"
variation 3169
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:938947137"
variation 3170
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:2115910499"
variation 3174
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446345598"
variation 3176
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:901114812"
variation 3177
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797057588"
variation 3181
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797057642"
variation 3187
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797057696"
variation 3188
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:576737071"
variation 3189
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:2115910604"
variation 3195
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797057792"
variation 3199
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1369822644"
variation 3203
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1323584028"
variation 3205..3208
/gene="CLDN12"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1797057932"
variation 3207
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797057981"
variation 3211
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:745956902"
variation 3216
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:2115910679"
variation 3231
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797058094"
variation 3237
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797058145"
variation 3238
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1797058213"
variation 3239
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1389192782"
variation 3240
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797058352"
variation 3242
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797058424"
variation 3246
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1158273121"
variation 3248..3252
/gene="CLDN12"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1797058581"
variation 3261
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797058652"
variation 3264
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316883037"
variation 3265
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1405844726"
variation 3267
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:894169464"
variation 3272
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797059374"
variation 3273
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1192064772"
variation 3276
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1466524143"
variation 3280
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797059508"
variation 3282
/gene="CLDN12"
/replace="c"
/replace="g"
/db_xref="dbSNP:1012602241"
variation 3283
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1215674137"
variation 3289
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315698081"
variation 3290
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1280072272"
variation 3301
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:545732176"
variation 3302
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797059696"
variation 3304
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1346619779"
variation 3309
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1300801034"
variation 3313
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797059831"
variation 3317
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797059890"
variation 3318
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797059938"
variation 3319
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1436906132"
variation 3321
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1733723153"
variation 3322
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:17863096"
variation 3324
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:888211500"
variation 3326
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1004331449"
variation 3340
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1266722145"
variation 3341
/gene="CLDN12"
/replace=""
/replace="t"
/db_xref="dbSNP:1178254743"
variation 3342..3343
/gene="CLDN12"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1435418017"
variation 3342
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797060319"
variation 3343
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797060420"
variation 3348
/gene="CLDN12"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1023940250"
variation 3356
/gene="CLDN12"
/replace="g"
/replace="t"
/db_xref="dbSNP:1797060544"
variation 3360
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797060581"
variation 3362..3364
/gene="CLDN12"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1451611393"
variation 3363
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1562970685"
variation 3369
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797060727"
variation 3374
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1584670878"
variation 3375
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797060823"
variation 3379
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:531134386"
variation 3380
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797060935"
variation 3381
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1584670890"
variation 3382
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797061029"
variation 3383
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:780262130"
variation 3388
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:980379733"
variation 3391
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:747178785"
variation 3392
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:920807704"
variation 3393
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1485051455"
variation 3403..3405
/gene="CLDN12"
/replace="ata"
/replace="atata"
/db_xref="dbSNP:1277638017"
variation 3405
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1230123160"
variation 3408
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1489120300"
variation 3411
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1797061859"
variation 3416
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:965175977"
variation 3420
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1797061965"
variation 3426
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:1294523360"
variation 3428
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797062126"
variation 3429
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:530747526"
variation 3431
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797062284"
variation 3434
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:2115911443"
variation 3436
/gene="CLDN12"
/replace="a"
/replace="c"
/db_xref="dbSNP:998090009"
variation 3437
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:543242983"
variation 3439
/gene="CLDN12"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:561267693"
variation 3440
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1028179618"
variation 3442
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:953942632"
variation 3448
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1584670950"
variation 3449
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:184005906"
variation 3450
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:914516784"
variation 3452
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797062749"
variation 3453
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797062801"
variation 3458
/gene="CLDN12"
/replace="a"
/replace="t"
/db_xref="dbSNP:1414150112"
variation 3462
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1475207043"
regulatory 3469..3474
/regulatory_class="polyA_signal_sequence"
/gene="CLDN12"
/note="hexamer: ATTAAA"
variation 3471
/gene="CLDN12"
/replace="c"
/replace="t"
/db_xref="dbSNP:1797062957"
variation 3472..3475
/gene="CLDN12"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1797063002"
variation 3475
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:17866176"
variation 3476
/gene="CLDN12"
/replace=""
/replace="g"
/db_xref="dbSNP:1311180978"
variation 3476
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:1797063171"
variation 3477
/gene="CLDN12"
/replace="a"
/replace="g"
/db_xref="dbSNP:776979988"
variation 3482..3486
/gene="CLDN12"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1797063331"
polyA_site 3490
/gene="CLDN12"
/note="major polyA site"
ORIGIN
gggaacgcacttcctgggacgctgagagggagacgctccaagaggctcctcagtgtgggcgagtaaaatgccctgcgtgtgagaagcaggctcagattattgctactctgtattcagatcttcatgtgtctcttctaagctgaataaagctgttttggaactgtcaggtacctcaaagctctgactgacagtactccacaagcttgcctgccatgggctgtcgggatgtccacgcagccacagtcctttccttcctgtgtggaatcgcctcagtagcaggcctctttgcagggactctgcttcccaactggagaaaattacgattgatcacattcaacagaaacgagaagaacctgactgtttacacaggcctgtgggtgaaatgtgcccggtatgacgggagcagtgactgcctgatgtacgacactacttggtactcatcagttgaccagctggacctgcgtgtcctccagtttgccctacccctcagcatgctgatcgccatgggtgccctgctgctctgcctgattggaatgtgcaacactgccttcaggtcctcggtgcccaacatcaaactggccaagtgtctggtcaatagtgcaggttgccacctggtggctgggctgctatttttcctggcaggtactgtgagcctctccccatctatctgggtcatcttttataacatccatctgaacaagaagtttgagccagtcttttcatttgactatgcagtgtatgtcactattgctagtgctgggggcctgtttatgacttcccttatactatttatttggtattgtacatgcaaatctttgccttctcctttctggcaaccattgtactcccatccacccagtatgcatacttactcacagccctattcagcacgctctcgcctctctgccattgaaattgacattccagtagtttcacacaccacttaatggggaaatagttaattgttaaagaaaacttcttgtagcctcacattccccttgtgcaaagagctcttttggacctacatacattttcctttgtttttgaccaatcaatgaagccaaatttatatgtcctagtagaatgaagtgctgctagtttttatgagaagtatattatattaaatgtgaattttttaaattttgcttcttatactggaaggaattttagccttcatattgatatctaattaattatttaagtggaagaggcctgcatcacaattgaggtaatgtagagcaacatgttaaagaatgatggttagcagaagctgttgtatacaatcttcatgaaaatttcagtgtgtatttttctttttctataatacctttaactgcaaagaaaaggcagtttcaaatataagaaatttatttcaggtaagggtaatattttaatagtagtcaataatctagcttaaggctgtaactcttctatcggggctaattgtatgaataggtgtcagtatgttgaagattactttcttttgtgactttcttctacctcatgccactgtttaaaagtaaaacgtattttaacgatgttagaataagactaccattctaaatatcacctacttatgaataacatgtaataatttttaacattaatgattccataaattgtattattgggattagaatgtgctttatgacaggttagtgtttcctctgaggcagaaaactcttttttggagatatcttccatcaagcagtactcgtgcccatatacaatctcttagtggctaggagaaataaataaaagggccataatggtttgttctctttcagacataatttagtaggggacaagaagtctgttcttcagtgagtacactagagatttactctggtgactgccttttgagttatgggtgaagtaaggtatggctttaccataaccttgattcattcacccttgattcatttctcgcccccgtcactgattatttccttgagcatatatctctgcctaacactttagtaggtgctatagaggatacatgaaaagtatgagatctggttccatccagtaagacattttaatagagaagatcaaaatgttacctggcagttggggaataatctgacttcgttggcagttggccttaacttcttaatcattgatccaggaatatttcaaccagagacacaactttctggcagacagacaaattgtacaacaccaacaatatcctggaccttgaaattctgtttacttcagtccattgtatcctttaaggcacctgtgctagcctagattttgtaataacactgatttatgagaatggacaaaagtggtagggaaattgttccctctccacttctgaaagtatgatgatgtattaaggatggaggagttattaaaaatgtctcttctgatgaggtaacaattagatgaaaccatgttaaagctgagatgaacacttagaaattcagggatattgggtctttagccttatgaatttgagctgcttatttaattggtgtaatttactacatattagtactatattcgtaaggattttttattaaccattacagattttacaaacagctagttatatggtaaacagattattatgcctttttgcaattctgaatatgattctagtatttgtgtagatgtatttggtactttttcccctaattccaacactagtttatatatatagcgaataaatctagttgtataaatttttaaatgccgtcagtagaaagcacacaaggttatgatttttttaattactggcttctgatttctttcacttctgatccttttcctttttctcagatgtagctgagtcttgatcattttaagacaacgatgggtagaattttgagattaatgttaattttccctttttgttaatttcagtcccctctcactatgcttttgtccagaaggatcaagaattctaccatcccttgggtctttgtgtataaacaatgttaaataaaggtagactcagtctttaagatattagacagtttttttagtccatgggattgtaaatataaacattaactttcctataagaatattttggctttgtaatctatagcctcaaattggtatttattatggattcactagacaaacagctgtttccttattgtcttttttctttagtgtttctgatttgctatcagtagctgtttttaaagccgtccaaggaaaataattatttacagtttttgaagtcacttttgagccctcatcaagctctcattgtgatgggagggatacctttttgttgttaaaagcctattattgttaaaggccttttatggaaaccaacttggaaaacaaccttaaatgtggatgtatcagatttggtttatccagccatgggagagaaaacaaacctaagtttactttacttgtacatatacactacaatggatagtatatttgctgtaaactacaatgtaaaacctcaataaaagtgcgctgtacttcttaatgtttattaaaagatgtatttttacaa
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
[Full Text]